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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2065627Erstellt: 25. Oktober 2026

Triethylamine → 6-Chloro-2-[1-(naphthalen-2-ylcarbamoyl)-ethylamino]-quinoline-3-carboxylic acid

https://huagongshe.com/reaction/2065627

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktDL-Alanine-beta-naphthylamideHCID 98159—
Edukt2,6-Dichloroquinoline-3-carboxylic acidHCID 24266068—
Lösungsmittel1,4-DioxaneHCID 31275—
Produkt6-Chloro-2-[1-(naphthalen-2-ylcarbamoyl)-ethylamino]-quinoline-3-carboxylic acidHCID 4525475260%

Reaktionsbedingungen

Temperatur135 °C

Reaktionsschritte

A mixture of 2,6-dichloroquinoline-3-carboxylic acid (194 mg, 0.8 mmol), DL-alanine-β-naphthylamide (251 mg, 1 mmol) and triethylamine (900 mg, 8.9 mmol) in dioxane (1 mL) is stirred for 24 h at 135° C. in closed reaction vial. After evaporation of solvents in vacuo, the residue is acidified by addition of 2N HCl, and the precipitated solid is collected on filter, washed with water and recrystallized from MeOH-water to give the title compound (200 mg, 60%) as yellow needles.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08288549B2
Quelldatensatzuspto-grants-2012_10
ORD IDord-b9f374a02f3847068c962de208210b48
Quellennotizuspto-grants-2012_10